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Live Tinted Hueguard Skin Tint Zinc Oxide 132 mg/mL Lotion — NDC 82153-0192-04 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Live Tinted Hueguard Skin Tint Zinc Oxide 132 mg/mL Lotion — NDC 82153-192-04 (Billing 82153-0192-04)

by Live Tinted · 1 TUBE in 1 CARTON / 10 mL in 1 TUBE

This is a package of Live Tinted Hueguard Skin Tint Zinc Oxide 132 mg/mL Lotion from Live Tinted, marketed since Nov 2023 and currently FDA-listed.

NDC 82153-0192-04
🏷️ FDA NDC (as labeled) 82153-192-04 billing pads the product segment with a zero
This package
Contains10 mL in 1 tube Pack sizes2 compare ↓
Product page 82153-0192-02 Also comes in: 40 mL 82153-192-02
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 2026 · this listing last changed Jul 24, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →

This page is curated, coded, and maintained by

Compiled from public FDA, CMS, DailyMed, NADAC, and related drug data sources. Editorial policy

NDC database record

One package, one record: these facts belong to NDC 82153-192-04 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
82153 labeler · 192 product · 04 package
Package marketed since
Sep 13, 2024
Sample package
No — commercial package
Listing certified through
Dec 31, 2027
Barcode (UPC-A, from the NDC)
3 8215319204 8
FDA record last changed
Jul 24, 2026
⚠️
Other active recalls for Zinc Oxide (different manufacturers) — 6 · tap to view
These affect other manufacturers’ products for the same ingredient — not necessarily the exact NDC on this page.
Class II · Oct 31, 2025 — cGMP deviations (Blossom Pharmaceuticals) · FDA recall D-0212-2026
Class II · Oct 31, 2025 — cGMP deviations (Blossom Pharmaceuticals) · FDA recall D-0206-2026
Class II · Oct 31, 2025 — cGMP deviations (Blossom Pharmaceuticals) · FDA recall D-0202-2026
Class II · Oct 31, 2025 — cGMP deviations (Blossom Pharmaceuticals) · FDA recall D-0207-2026
Class II · Oct 31, 2025 — cGMP deviations (Blossom Pharmaceuticals) · FDA recall D-0209-2026
Class II · Oct 31, 2025 — cGMP deviations (Blossom Pharmaceuticals) · FDA recall D-0208-2026
Each entry is an official FDA enforcement report — look up any recall number in the FDA recall database ↗

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 82153-192-04
Product NDC 82153-192
11-digit billing NDC 82153019204
UNII SOI2LOH54Z
Application # M020
SPL Set ID 0ff39ab1-e8d3-cad9-e063-6394a90af0eb
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2023-11-28
Route TOPICAL
Dosage form LOTION
Substance ZINC OXIDE
Why two NDCs? The FDA registers this code as 82153-192-04 — a 5-3-2 layout, and that's what's printed on the package and shown on DailyMed. For insurance claims, every NDC is standardized to a uniform 11-digit 5-4-2 format by adding a zero to the product segment → 82153-0192-04. Same drug, same package — only the format differs.
Where does this data come from?
Identifiers from the FDA openFDA NDC Directory and Structured Product Labeling; RxCUI from RxNorm (NLM); GPI from Medi-Span; GCN / HIC / AHFS / legend from First Databank.

Clinical

🧪 What is this product?

This is a topical lotion containing zinc oxide, an inorganic mineral commonly used in over-the-counter sunscreen products to help block ultraviolet (UV) radiation from the sun. Zinc oxide functions as a physical sunscreen agent and is typically found in formulations intended for sun protection. As an OTC monograph drug, this product is marketed under FDA's established rules for sunscreen ingredients rather than through individual product approval.

Supplement & herbal interactions

Some supplements/herbs that may interact with Zinc oxide (OTC drug) — tap one for details:

Dimethylsulfoxide (dmso)Moderate Turpentine OilModerate AlchemillaMinor
🌿 Every supplement checked against Zinc oxide (OTC drug) (3 interactions) — ranked by severity →
Where does this data come from?
Plain-language summary from MedlinePlus (U.S. National Library of Medicine); supplement & herbal interactions and nutrient depletion data from the Natural Medicines database; our full guide is HelloPharmacist editorial content.

Pricing

A drug doesn't have one price. Each row is a different public payment system, and none is what you'd pay at the counter — that depends on your insurance. The ⓘ on each row explains what it measures.

Price systemPer gPer package
Retail pharmacies payNADAC · weekly Not in the retail survey — common for institutional, discontinued, or low-volume packs.
Medicaid paysCMS SDUD · 12 mo No recent Medicaid claims on file for this NDC — rare and low-volume NDCs are suppressed in the public data.
Medicare drug plans payPart D · quarterly No Part D plan price is available for this NDC in our data.
ℹ️
No price is published for this exact package yet. CMS surveys NADAC per package size, so a different pack of the same drug often has one.
Try another pack size: 40 mL
Where does this data come from?
NADAC (National Average Drug Acquisition Cost) is the CMS weekly pharmacy-acquisition-cost survey — what pharmacies pay. ASP (Average Sales Price) is the CMS Medicare Part B drug-payment file, published quarterly. Medicaid pays is computed by us from CMS State Drug Utilization Data (total reimbursed ÷ units, trailing 12 months) — gross of rebates and inclusive of dispensing fees, so it reflects what Medicaid paid, not an acquisition cost. Medicare drug plans pay is the median negotiated point-of-sale unit cost across plans listing this NDC in the CMS quarterly Prescription Drug Plan pricing files, before rebates. The VA pays is the federal contract price (FSS, and the statutory Big 4 ceiling where listed) from the VA National Acquisition Center pharmaceutical price file. All are free public government data; each measures a different payer, so the figures are not directly comparable.

Packaging — all sizes for this product

Package NDCDescription Marketing startMarketing endStatus
82153-0192-02 82153-192-02 Main listing 1 TUBE in 1 CARTON / 40 mL in 1 TUBE 2023-11-28 — Active
82153-0192-04 You're viewing this 1 TUBE in 1 CARTON / 10 mL in 1 TUBE 2024-09-13 — Active

Pack size FAQ

What quantity is in this package?
This package is listed by the FDA — 1 tube in 1 carton / 10 ml in 1 tube.
What NDC number is used to bill for this package of Live Tinted Hueguard Skin Tint Zinc Oxide 132 mg/mL Lotion?
Use the 11-digit billing form listed in the identifiers section of this page. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Indie Lee Daily Primer 132 mg/mL 78870-0245-02 America 1 bottle — — FDA listed —
Ilia Super Serum Skin Tint (St12.5 Ramla Bay) 132 mg/mL 81110-0054-02 Ilia, 1 bottle — — FDA listed —
Ilia Super Serum Skin Tint (St4 Formosa) 132 mg/mL 81110-0753-02 Ilia, 1 bottle — — FDA listed —
Golden Ray Sunscreen (Deep Tinted) 132 mg/mL 82184-1350-02 A-Frame 1 bottle — — Discontinued —
Daybird Tinted Skincare (SHADE 2) 132 mg/mL 82417-1063-02 Resette, 1 bottle — — FDA listed —
Ciele Bronze and Protect 132 mg/mL 83103-2255-02 Ciele 1 bottle — — FDA listed —
DRMTLGY Lip Silk - Bold 132 mg/mL 83286-0140-02 DRMTLGY 1 bottle — — FDA listed —
Alleyoop Sun Serum Lip Oil 132 mg/mL 84830-2107-02 NewAlley 1 bottle — — Discontinued —
Sunsolve MD Volumize and Condition Lip 132 mg/mL 84878-0107-02 Sunsolve 1 bottle — — FDA listed —
Sunsolve MD Mineral Shade Bronzite 004 132 mg/mL 84878-0404-02 Sunsolve 1 bottle — — FDA listed —
Sunsolve MD Mineral Shade Garnet 005 132 mg/mL 84878-0405-02 Sunsolve 1 bottle — — FDA listed —
Daily Essential Lip Oil Scarlet Bloom 132 mg/mL 84891-1842-01 Solarium 10 ml — — FDA listed —
Yon-Ka 50 Mineral Fluid 132 mg/mL 51191-2667-02 Laboratoire 1 tube — — FDA listed —
PUR 4-in-1 Skin Tint LG3 132 mg/mL 67345-0051-00 PUR 1 bottle — — FDA listed —
Ilia Super Serum Skin Tint (St7 Diaz) 132 mg/mL 81110-0755-02 Ilia, 1 bottle — — FDA listed —
Bloomeffects Tulip Dew 132 mg/mL 82548-2193-04 Bloomeffects 1 bottle — — FDA listed —
Bloomeffects Tulip Dew Bronze 132 mg/mL 82548-2768-02 Bloomeffects 1 bottle — — FDA listed —
Melan RX 132 mg/mL 82635-0403-01 Melan 45 ml — — FDA listed —
Inde Wild 132 mg/mL 83054-1502-02 Inde 1 bottle — — FDA listed —
DRMTLGY Lip Silk - Soft 132 mg/mL 83286-0139-02 DRMTLGY 1 bottle — — FDA listed —
Blume Sunburst Sunscreen 132 mg/mL 83656-2106-02 Blume 1 bottle — — FDA listed —
Daily Essential Lip Oil Blushing Nude 132 mg/mL 84891-2107-01 Solarium 10 ml — — FDA listed —
Skin Metal Stealth 132 mg/mL 87098-0236-02 Skin 1 bottle — — FDA listed —
Knesko Skin The Sunscreen 132 mg/mL 87407-0236-02 Knesko, 1 bottle — — FDA listed —
PUR 4-in-1 Skin Tint DG6 132 mg/mL 67345-0057-00 PUR 1 bottle — — FDA listed —
Ilia Super Serum Skin Tint (St9.5 Baikal) 132 mg/mL 81110-0052-02 Ilia, 1 bottle — — FDA listed —
Ilia Super Serum Skin Tint (St17.5 Perissa) 132 mg/mL 81110-0059-02 Ilia, 1 bottle — — FDA listed —
Ilia Super Serum Skin Tint (St19 Lovina) 132 mg/mL 81110-0060-02 Ilia, 1 bottle — — FDA listed —
Ilia Super Serum Skin Tint (St6 Ora) 132 mg/mL 81110-0691-02 Ilia, 1 bottle — — FDA listed —
Ilia Super Serum Skin Tint (St1 Rendezvous) 132 mg/mL 81110-0750-02 Ilia, 1 bottle — — FDA listed —
Ilia Super Serum Skin Tint (St9 Paloma) 132 mg/mL 81110-0757-02 Ilia, 1 bottle — — FDA listed —
Golden Rays Sunscreen (Light Tinted) 132 mg/mL 82184-1351-02 A-Frame 1 bottle — — Discontinued —
Daybird Tinted Skincare (SHADE 1) 132 mg/mL 82417-1062-02 Resette, 1 bottle — — FDA listed —
Hanalei Face Moisturizing 132 mg/mL 82915-2133-02 Hanalei 1 tube — — FDA listed —
Balmere Mineral Sunscreen Moisturizer Primer 132 mg/mL 83241-1039-02 Balmere 1 bottle — — FDA listed —
Iris and Romeo Weekend Skin 132 mg/mL 83247-1321-02 Iris 1 tube — — FDA listed —
Iris and Romeo Weekend Skin Warm Glow 132 mg/mL 83247-1838-02 Iris 1 tube — — FDA listed —
Alleyoop Sun Serum Lip Oil - Daylight 132 mg/mL 84830-7210-02 NewAlley 1 bottle — — FDA listed —
Sunsolve MD Correct and Fade 132 mg/mL 84878-0200-02 Sunsolve 1 bottle — — FDA listed —
Solarium Daily Essentials Luminizing Glow Drops 132 mg/mL 84891-2191-01 Solarium 30 ml — — FDA listed —
Oiana Mineral Sunscreen Drops 132 mg/mL 87342-2368-02 Oiana 1 bottle — — FDA listed —
PUR 4-in-1 Skin Tint TN7 132 mg/mL 67345-0055-00 PUR 1 bottle — — FDA listed —
Riversol Daily Glow Mineral Tinted 132 mg/mL 72019-2035-02 Riversol 1 bottle — — FDA listed —
Volition Prismatic Luminizing Shield 132 mg/mL 72577-0624-02 Volition 1 bottle — — FDA listed —
Ilia Super Serum Skin Tint (St10 Porto Ferro) 132 mg/mL 81110-0758-02 Ilia, 1 bottle — — FDA listed —
Ilia Super Serum Skin Tint (St12 Kokkini) 132 mg/mL 81110-0760-02 Ilia, 1 bottle — — FDA listed —
Ilia Super Serum Skin Tint (St16 Pavones) 132 mg/mL 81110-0764-02 Ilia, 1 bottle — — FDA listed —
KINLO Golden Rays Sunscreen 132 mg/mL 82184-4480-02 A-Frame 1 bottle — — Discontinued —
Daybird Tinted Skincare (SHADE 3) 132 mg/mL 82417-1064-02 Resette, 1 bottle — — FDA listed —
Ciele Tint and Protect 132 mg/mL 83103-1819-02 Ciele 1 bottle — — FDA listed —
Duette Tinted 132 mg/mL 84123-2034-02 Skin 1 bottle — — FDA listed —
Daily Essential Face Moisturizer 132 mg/mL 84891-2185-01 Solarium 60 ml — — FDA listed —
Sonni SunDay Serum 132 mg/mL 85260-0282-02 Sonni 1 bottle — — FDA listed —
Peachy Tinted Facial Sunscreen 132 mg/mL 85600-2034-02 Peachy 1 bottle — — FDA listed —
Peachy Mineral Facial Sunscreen 132 mg/mL 85600-2368-02 Peachy 1 bottle — — FDA listed —
Odacite Nourishing Lip Serum - Bubble Gum 132 mg/mL 82088-0871-02 Odacite 1 bottle — — FDA listed —
SOL Science The Fifty 132 mg/mL 83282-0139-02 Beauty 1 bottle — — FDA listed —
DRMTLGY Lip Silk 132 mg/mL 83286-0213-02 DRMTLGY 1 bottle — — Discontinued —
Riversol Tinted Lip Oil - Poppy 132 mg/mL 63931-8421-02 Solesence, 1 tube — — FDA listed —
PUR 4-in-1 Skin Tint DP3 132 mg/mL 67345-0056-00 PUR 1 bottle — — FDA listed —
Naked Sundays BeautyScreen Peptide Foundation Tint 132 mg/mL 81104-0664-02 Naked 1 tube — — FDA listed —
Ilia Super Serum Skin Tint (St0.5 Skye) 132 mg/mL 81110-0049-02 Ilia, 1 bottle — — FDA listed —
Ilia Super Serum Skin Tint (St2.5 Sombrio) 132 mg/mL 81110-0050-02 Ilia, 1 bottle — — FDA listed —
Ilia Super Serum Skin Tint (St11 Matira) 132 mg/mL 81110-0759-02 Ilia, 1 bottle — — FDA listed —
Ilia Super Serum Skin Tint (St13 Kamari) 132 mg/mL 81110-0761-02 Ilia, 1 bottle — — FDA listed —
Ilia Super Serum Skin Tint (St15 Porto Covo) 132 mg/mL 81110-0763-02 Ilia, 1 bottle — — FDA listed —
Bloomeffects Tulipscreen Hydrating Lip Oil Tulipy Pink 132 mg/mL 82548-2340-02 Bloomeffects 1 bottle — — FDA listed —
Covey Sun and Done Daily Moisturizing 132 mg/mL 83338-0087-02 Covey 1 tube — — FDA listed —
Vaihea Protect Clean SPF Drops 132 mg/mL 83395-0050-02 Vaihea 1 bottle — — FDA listed —
Organys Derma Made 132 mg/mL 83612-0330-01 Organys 45 ml — — Discontinued —
Organys Open Formula Sheer 132 mg/mL 83612-1391-01 Organys 45 ml — — FDA listed —
Green Envee Radiance Sheer 132 mg/mL 83678-2726-02 Green 1 bottle — — FDA listed —
Alleyoop Sunsational Broad Spectrum 132 mg/mL 84830-2431-02 NewAlley 1 tube — — Discontinued —
Sunsolve MD Firm and Replenish 132 mg/mL 84878-0199-02 Sunsolve 1 bottle — — FDA listed —
Sunsolve MD Calm and Revitalize 132 mg/mL 84878-0654-02 Sunsolve 1 bottle — — FDA listed —
Riversol Daily Glow Mineral Untinted 132 mg/mL 72019-2033-02 Riversol 1 bottle — — FDA listed —
Ilia Super Serum Skin Tint (St6.5 Kai) 132 mg/mL 81110-0051-02 Ilia, 1 bottle — — FDA listed —
Ilia Super Serum Skin Tint (St12.75 Papakolea) 132 mg/mL 81110-0055-02 Ilia, 1 bottle — — FDA listed —
Ilia Super Serum Skin Tint (St13.5 Rialto) 132 mg/mL 81110-0056-02 Ilia, 1 bottle — — FDA listed —
Ilia Super Serum Skin Tint (St16.5 Jardin) 132 mg/mL 81110-0058-02 Ilia, 1 bottle — — FDA listed —
Ilia Super Serum Skin Tint (St5 Bom Bom) 132 mg/mL 81110-0754-02 Ilia, 1 bottle — — FDA listed —
Odacite Nourishing Lip Serum - True Nude 132 mg/mL 82088-0875-02 Odacite 1 bottle — — FDA listed —
Live Tinted Hueguard Skin Tint 132 mg/mLthis 82153-0192-04 Live 1 tube — — FDA listed —
Bloomeffects Tulipscreen Hydrating Lip Oil 132 mg/mL 82548-2341-02 Bloomeffects 1 bottle — — Discontinued —
Organys Derma Made Sheer 132 mg/mL 83612-1039-01 Organys 45 ml — — FDA listed —
Sunsolve MD Mineral Shade Quartz 001 132 mg/mL 84878-0401-02 Sunsolve 1 bottle — — FDA listed —
PUR 4-in-1 Skin Tint MN3 132 mg/mL 67345-0052-00 PUR 1 bottle — — FDA listed —
Odacite Flex Perfecting Mineral Drops Tinted Sunscreen 132 mg/mL 82088-0214-02 Odacite 1 bottle — — FDA listed —
Daybird Tinted Skincare (SHADE 4) 132 mg/mL 82417-1065-02 Resette, 1 bottle — — FDA listed —
Organys Derma Made 132 mg/mL 83612-0282-01 Organys 45 ml — — Discontinued —
Agent Natuer holi (sun) dewy tinted skin drops 132 mg/mL 83633-2063-02 Agent 1 bottle — — FDA listed —
Guise Tinted Drops 132 mg/mL 83827-1208-02 Donis 1 bottle — — FDA listed —
Duette Untinted 132 mg/mL 84123-2033-02 Skin 1 bottle — — FDA listed —
Depology Essential Mineral UV Care 132 mg/mL 84133-1039-02 Depology 1 tube — — FDA listed —
Morning Person Daily Repair Protect Moisturizer 132 mg/mL 84846-1039-02 Morning 1 tube — — FDA listed —
Sunsolve MD Mineral Shade Amber 002 132 mg/mL 84878-0402-02 Sunsolve 1 bottle — — FDA listed —
Daily Essential Lip Oil Dusty Rose 132 mg/mL 84891-2181-01 Solarium 10 ml — — FDA listed —
Riversol Tinted Lip Oil - Poppy 132 mg/mL 72019-1842-02 Riversol 1 tube — — FDA listed —
Ilia Super Serum Skin Tint (St11.5 Morgat) 132 mg/mL 81110-0053-02 Ilia, 1 bottle — — FDA listed —
Ilia Super Serum Skin Tint (St14.5 Honopu) 132 mg/mL 81110-0057-02 Ilia, 1 bottle — — FDA listed —
Ilia Super Serum Skin Tint (St3 Balos) 132 mg/mL 81110-0752-02 Ilia, 1 bottle — — FDA listed —
Ilia Super Serum Skin Tint (St8 Shela) 132 mg/mL 81110-0756-02 Ilia, 1 bottle — — FDA listed —
Ilia Super Serum Skin Tint (St14 Dominica) 132 mg/mL 81110-0762-02 Ilia, 1 bottle — — FDA listed —
Odacite Nourishing Lip Serum - Jazzy Berry 132 mg/mL 82088-0876-02 Odacite 1 bottle — — FDA listed —
Daybird 4-in-1 Skin Tint Serum 132 mg/mL 82417-1210-02 Resette, 1 bottle — — FDA listed —
Green Envee Sun Shield Serum 132 mg/mL 83678-2049-02 Green 1 bottle — — Discontinued —
Sunsolve MD Mineral Shade Agate 003 132 mg/mL 84878-0403-02 Sunsolve 1 bottle — — FDA listed —
PUR 4-in-1 Skin Tint MN4 132 mg/mL 67345-0053-00 PUR 1 bottle — — FDA listed —
PUR 4-in-1 Skin Tint TN2 132 mg/mL 67345-0054-00 PUR 1 bottle — — FDA listed —
Ilia Super Serum Skin Tint (St2 Tulum) 132 mg/mL 81110-0751-02 Ilia, 1 bottle — — FDA listed —
Ilia Super Serum Skin Tint (St17 Miho) 132 mg/mL 81110-0765-02 Ilia, 1 bottle — — FDA listed —
Ilia Super Serum Skin Tint (St18 Mali) 132 mg/mL 81110-0766-02 Ilia, 1 bottle — — FDA listed —
DMK Ultrascreen Mineral Sunscreen 132 mg/mL 81537-0282-02 Danne 1 bottle — — FDA listed —
Odacite Mineral Drops Sheer Sunscreen 132 mg/mL 82088-0285-02 Odacite 1 bottle — — FDA listed —
KINLO Golden Rays Sunscreen (Medium Tinted) 132 mg/mL 82184-1173-02 A-Frame 1 bottle — — Discontinued —
Bloomeffects Tulipscreen Hydrating Lip Oil Barely 132 mg/mL 82548-1234-02 Bloomeffects 1 bottle — — FDA listed —
Bloomeffects Tulipscreen Hydrating Lip Oil Fruit Punch 132 mg/mL 82548-2350-02 Bloomeffects 1 bottle — — FDA listed —
Bloomeffects Tulipscreen Hydrating Lip Oil Mauve Moment 132 mg/mL 82548-2601-02 Bloomeffects 1 bottle — — FDA listed —
Aspen Islanders Sheer Mineral Sport 132 mg/mL 83382-1005-02 Aspen 1 tube — — FDA listed —
Organys Derma Made 132 mg/mL 83612-0403-01 Organys 45 ml — — FDA listed —
Sunsolve MD Mineral Shade Onyx 006 132 mg/mL 84878-0406-02 Sunsolve 1 bottle — — FDA listed —
Sunsolve MD Balance and Clear 132 mg/mL 84878-0997-02 Sunsolve 1 bottle — — FDA listed —
Sunsolve MD Detox and Shield 132 mg/mL 84878-0998-02 Sunsolve 1 bottle — — FDA listed —
Skin Metal Green Stealth 132 mg/mL 87098-0270-02 Skin 1 bottle — — FDA listed —
BEAUTY SHIELD BROAD SPECTRUM SUNSCREEN (Napoleon Perdis) 132 mg/mL 51386-0291-02 Napoleon 1 tube — — FDA listed —
PUR 4-in-1 Skin Tint LN2 132 mg/mL 67345-0050-00 PUR 1 bottle — — FDA listed —
Omnilux Mineral Facial Sunscreen 132 mg/mL 83866-1762-02 The 1 bottle — — FDA listed —
About this product: other versions of the same ingredient, strength and form are listed above, least expensive first, with FDA equivalence ratings where available.
Where does this data come from?
Equivalents are other NDCs of the same ingredient, form and route from the openFDA NDC Directory, ranked least-expensive-first by NADAC. Therapeutic-equivalence (AB) ratings come from the FDA Orange Book; biologics use the FDA Purple Book for biosimilar & interchangeable status.

Availability & generic status

🏛️
2023
On the market since
Nov 2023
📍
2026
Currently FDA-listed
3 years listed
🔒
·
No generic listed yet
brand only
ℹ️No FDA-approved generic found

We did not find an FDA-approved generic match for this exact strength, form and route.

Where does this data come from?
Patents and exclusivity from the FDA Orange Book (small-molecule drugs), refreshed from public FDA data. Generic launch timing is an estimate, not a guarantee.

What it looks like

Color brown
One label can cover several strengths, so colors may be combined — always confirm a loose pill against the dispensed prescription label or a pharmacist.
Where does this data come from?
Physical description (imprint, shape, color, scoring, coating) from this product’s FDA Structured Product Labeling (SPL), mirrored from DailyMed / openFDA.

Inactive Ingredients / Excipients

Inactive ingredients, also called excipients, are components of the drug product other than the active ingredient. They may include fillers, dyes, coatings, preservatives, flavors, or other formulation ingredients.

💡 Tap an ingredient (hover on desktop) to see what it is and why it’s used.

  • UNII 105S6I733Z
    A natural oil extracted from chamomile and other plants. It acts as a fragrance and flavoring agent to improve the taste and smell of the medicine.
  • UNII A9EJ3J61HQ
    A synthetic liquid derived from benzoic acid and long-chain alcohols. It functions as a solvent and penetration enhancer in topical formulations, helping active ingredients dissolve and absorb into the skin.
  • UNII 344S277G0Z
    Allantoin is a naturally derived compound that helps soften and soothe skin. In medicines, it works as a skin-conditioning agent and may help support wound healing and reduce irritation in topical formulations.
  • UNII 5QB0T2IUN0
    Aluminum hydroxide is a white powder mineral compound used as an antacid ingredient in some formulations. It works as a buffer and pH regulator to help neutralize stomach acid in the medicine.
  • UNII QN83US2B0N
    Ascorbyl palmitate is a fat-soluble form of vitamin C used as an antioxidant in medicines. It prevents oils and fats in the product from breaking down and becoming less stable over time.
  • UNII 2EH13UN8D3
    A synthetic compound used as a solvent and penetration enhancer in topical formulations. It helps dissolve active ingredients and allows them to penetrate the skin more effectively.
  • UNII 114P5I43UJ
    A hydrocarbon oil derived from petroleum, containing 13 to 15 carbon atoms per molecule. It serves as a lubricant and glidant in tablets and capsules to reduce friction during manufacturing and improve powder flow.
  • UNII 00YIU5438U
    Caprylyl glycol is a clear liquid derived from coconut oil. In medicines, it acts as a humectant to retain moisture, a preservative booster to prevent microbial growth, and a solvent to help dissolve or mix other ingredients.
  • UNII 4828G836N6
    A plant-derived oil mixture from coconut that acts as an emollient and solvent. It helps dissolve or carry active ingredients and improves how the medicine spreads or absorbs in topical formulations.
  • UNII X687XDK09L
    A clay mineral processed to carry positive charges, used as a thickener and suspending agent in liquid medicines. It helps keep solid particles evenly distributed throughout the product.
  • UNII 1K09F3G675
    Ferric oxide red is an inorganic iron compound used as a colorant in medicines. It gives tablets, capsules, or other dosage forms a red or reddish tint for identification and appearance.
  • UNII EX438O2MRT
    Ferric oxide yellow is a naturally occurring iron compound used as a colorant in medications. It gives tablets, capsules, and other forms a yellow or golden hue for identification and appearance.
  • UNII XM0M87F357
    A dark iron oxide compound that gives medicines their black or dark color. It's used as a colorant in tablets and capsules to help identify the product and make it visually distinctive.
  • UNII PDC6A3C0OX
    Glycerin is a clear, thick liquid derived from plant oils or fats. It acts as a humectant to retain moisture, a sweetener, and a solvent in medications.
  • UNII T53SBG6741
    A plant-based oil extracted from sea buckthorn seeds. It's used as an emollient and skin-conditioning agent to soften the medicine's texture and improve how it feels or spreads on skin.
  • UNII M1SLX00M3M
    Isoamyl laurate is a synthetic ester made from isoamyl alcohol and lauric acid. It functions as an emollient and lubricant in topical formulations to help smooth and soften the skin.
  • UNII 1DI56QDM62
    A natural fatty substance from soybeans that helps mix oil and water-based ingredients together. It acts as an emulsifier and lubricant in medicines to improve texture and help the product break down properly in your body.
  • UNII N8F53B3R4R
    A synthetic humectant and solvent derived from propane. It draws and holds moisture in the formulation, helping keep the medicine stable and improving texture or flow in liquid and semi-solid products.
  • UNII GM2TDN9DZI
    A juice extract from physalis pubescens fruit, a plant in the nightshade family. It's used as a flavoring agent and natural coloring ingredient in medicines.
  • UNII 687U3PEB2Y
    A complex emulsifier made from glycerin and fatty acids. It helps blend oil and water-based ingredients together and improves the texture and stability of creams, lotions, and other formulated products.
  • UNII ETJ7Z6XBU4
    Silicon dioxide is a naturally occurring mineral used as a glidant and anti-caking agent. It helps powder ingredients flow smoothly and prevents clumping during manufacturing and storage.
  • UNII 451W47IQ8X
    Sodium chloride is common table salt. It's used in medicines as a buffer to maintain proper pH, as a filler to add bulk, or to adjust the osmotic balance in liquid formulations.
  • UNII 15FIX9V2JP
    Titanium dioxide is a bright white mineral powder commonly used as a colorant and opacifying agent. It makes pills and tablets white or lighter in color and helps make coatings non-transparent.
  • UNII R0ZB2556P8
    Tocopherol is a form of vitamin E derived from plant oils. It acts as an antioxidant in medicines to prevent oils and fats from breaking down and spoiling during storage.
  • UNII 059QF0KO0R
    Water is a liquid solvent that dissolves and mixes ingredients together in liquid medicines, syrups, and injections. It helps distribute the active drug evenly throughout the product.
  • UNII TTV12P4NEE
    Xanthan gum is a thickening and stabilizing ingredient made from fermented corn or other sugars. It's added to medicines to improve texture, prevent separation of liquids and solids, and help the product stay consistent.

26 inactive ingredients listed in the exact product block matched to this NDC.

Where does this data come from?
Data sourced from official FDA Structured Product Labeling (SPL) via DailyMed — ingredient classCode="IACT" elements from the exact product block matched by this NDC. Label-section narrative from DailyMed / the openFDA label index is shown separately when available.

Inactive ingredient FAQ

Are inactive ingredients the same for every manufacturer?
No. Inactive ingredients can differ by manufacturer, dosage form, strength, and package / product version.
Why might an inactive ingredient be missing?
Some SPLs do not provide a complete structured inactive-ingredient list, and older or unusual labels may only include the information in narrative text.
Can inactive ingredients matter?
Yes. They can matter for allergies, intolerances, dyes, gluten / lactose concerns, preservatives, and formulation differences — but confirm with a pharmacist or the manufacturer when it’s clinically important.

Manufacturer & labeler

LabelerLive Tinted
FDA applicationM020 (OTC MONOGRAPH DRUG)
Labeler code82153
First marketedNov 2023
Product typeHuman Otc Drug

More NDCs from Live Tinted labeler code 82153

The labeler markets the product; the application holder owns the FDA approval. They’re often the same company but can differ (e.g. a repackager or an authorized generic). A mailing address / phone appears here when the manufacturer includes it in the product’s FDA label (not all do).
Where does this data come from?
Labeler, application holder and registered establishment from the FDA openFDA NDC Directory and Drugs@FDA; address/contact from the product’s FDA label.

FDA label — Drug Facts FDA SPL

The complete FDA label for this product — the official Drug Facts labeling, verbatim, section by section. Jump with a chip, search within the label, or expand everything.
🎯 Indications and Usage ⏱️ Dosage and Administration ⚠️ Warnings 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose 📄 Keep Out of Reach of Children 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 8 words ▾

Live Tinted Hueguard Skin Tint Indication and Usage

⏱️ Dosage and Administration 8 words ▾

Live Tinted Hueguard Skin Tint Dosage and Administration

⚠️ Warnings 7 words ▾

Live Tinted Hueguard Skin Tint Warning Label

🧪 Active Ingredient 7 words ▾

Live Tinted Hueguard Skin Tint Active Ingredients

🧪 Inactive Ingredients 7 words ▾

Live Tinted Hueguard Skin Tint Inactive ingredients

🎯 Purpose 6 words ▾

Live Tinted Hueguard Skin Tint purpose

📄 Keep Out of Reach of Children 11 words ▾

Live Tinted Hueguard Skin Tint keep out of reach of children

📄 Package Label / Principal Display Panel 6 words ▾

Live Tinted Hueguard Skin Tint PDP

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗

Reported adverse events (FAERS)

Read carefully: FAERS reports are voluntary and unverified. Counts are not incidence, do not establish causation, are subject to reporting bias, and cannot be used to compare one drug to another. Shown for signal context only. Reports for Live Tinted Hueguard Skin Tint (this brand).

Top reported reactions

Macular Degeneration460
Pyrexia306
Nausea290
Pain282
Malaise261
Weight Decreased236
Therapeutic Product Effect Incomplete214

Reporter sex

1,941 reports

Serious outcomes

Death204
Life-threatening116
Disabling32
Reports over time (by year) — tap or hover for the count & year
2019 2021 2023 2026 229 0
Most recent year is provisional (FAERS lags ~3 months).
Where does this data come from?
Adverse-event reports from the FDA Adverse Event Reporting System (FAERS) via openFDA. FAERS reports are voluntary and unverified — counts are not incidence and don’t establish causation.

About this NDC listing & data coverage

Over-the-counter (OTC) product
What data is (and isn’t) available for this NDC — tap to expand
NDC identity (package / product / labeler codes) ✓ Available
Labeler ✓ Available
Product & package description ✓ Available
Marketing category & status ✓ Available
Active ingredient / dosage form / route ✓ Available
FDA label (SPL via DailyMed) ✓ Available
Package photos ✓ Available
Inactive ingredients (structured) ✓ Available
NADAC pharmacy acquisition price (CMS) — Not published for this NDC CMS publishes NADAC only for NDCs reported in its retail-pharmacy survey.
Orange Book / therapeutic-equivalence data — Not published for this NDC Applies only to products approved under an NDA/ANDA; many listings are out of scope.
HCPCS J-code billing crosswalk — Not published for this NDC Most self-administered / retail products have no J-code — that is normal.
Medicaid utilization (CMS SDUD) — Not published for this NDC CMS reports utilization only for NDCs with Medicaid claims above its privacy threshold.
“Not published” reflects what the public FDA / CMS / NLM sources provide for this exact package code — it is a property of the data feeds, not a judgment about the product.

Questions about this listing

Is this NDC FDA-approved?
An NDC listing does not by itself establish FDA approval — the NDC Directory records that a product is listed with FDA, not that it was reviewed and approved. This listing's marketing category is "Otc Monograph Drug". Products approved under an application carry an NDA, ANDA, or BLA number.
Why is there no price listed?
The pricing shown on our NDC pages comes from CMS NADAC, a voluntary survey of retail community pharmacy invoices. CMS does not publish a NADAC for every NDC — packages outside the retail survey (institutional and hospital products, bulk packages, discontinued items, and many OTC items) may never receive one. A missing price reflects the survey's scope, not this product's actual cost, and does not mean the product is free or unavailable.
Is the NDC printed on the package the same as the 11-digit billing NDC?
Yes, they identify this exact package in different formats. The form printed on the packaging and shown on DailyMed is the one the FDA registered. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero and the dashes are dropped. The Identity section at the top of this page lists each form of this code.
Is this package still being marketed?
Yes, per the latest FDA NDC Directory data on this page: this package is listed as actively marketed, with no marketing end date reported by Live Tinted. Listing status can change — the directory data on this page refreshes weekly.
Does this product come in other package sizes?
Yes — the FDA directory lists 1 other package presentation of this same product, including 1 tube (82153-0192-02). Each has its own NDC and its own page — see the package list near the top of this page.
Who lists this product with the FDA?
Live Tinted is the labeler of record for this NDC — the company under whose FDA-assigned code the package is listed. The labeler may be the manufacturer itself or a distributor marketing the product under its own code.
Do I need a prescription for this product?
This NDC is listed with FDA as an over-the-counter product, so it does not require a prescription. Follow the package directions, and ask your pharmacist if you are unsure whether it is right for you.
This page identifies an FDA-listed package (the NDC) and reports public regulatory and pricing data about the listing. It is reference information, not a medical recommendation — talk to your pharmacist or prescriber about your own medication.
Where does this data come from?
Listing facts (marketing category, packager status, marketing dates) from the FDA openFDA NDC Directory; label availability from DailyMed; pricing coverage from CMS NADAC; equivalence scope from the FDA Orange Book.
← 82153-0001-50 · Live 82153-0271-00 · Live →
For educational and professional reference only — not medical advice. Pricing reflects published NADAC and CMS ASP (free public data) and may differ from your acquisition cost; always verify before billing or dispensing.