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Target Up and Up Daily Moisturizing Dimethicone 12 mg/mL Lotion, 85 mL — NDC 11673-087-18 (Billing 11673-0087-18)

by TARGET CORPORATION · 85 mL in 1 TUBE

This is a package of 85 mL of Target Up and Up Daily Moisturizing Dimethicone 12 mg/mL Lotion from TARGET CORPORATION, marketed since May 2009 and currently FDA-listed. It is the main listing for this product, which comes in 3 package sizes.

NDC 11673-0087-18
🏷️ FDA NDC (as labeled) 11673-087-18 billing pads the product segment with a zero
This package
Contains85 mL Pack sizes3 compare ↓
Main listing for product 11673-087 · Also comes in: 2 bottles 11673-087-98 532 ml 11673-087-43
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

⚠️
Other active recalls for Dimethicone (different manufacturers) — 1 · tap to view
These affect other manufacturers’ products for the same ingredient — not necessarily the exact NDC on this page.
Class II · Jun 11, 2026 — Failed Impurities/Degradation Specifications; Formaldehyde levels exceeded specification. (BioMed Laboratories, LLC.) · FDA recall D-0663-2026
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) 11673-087-18
Product NDC 11673-087
11-digit billing NDC 11673008718
RxCUI 876980
UNII 92RU3N3Y1O
Application # M016
SPL Set ID f118e0eb-1e66-50ab-e053-2995a90a2cb9
Physiologic effect Skin Barrier Activity
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2009-05-01
Route TOPICAL
Dosage form LOTION
Substance DIMETHICONE
Quick answers
  • RxCUI (RxNorm): 876980
Why two NDCs? The FDA registers this code as 11673-087-18 — 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 → 11673-0087-18. 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.

RxNorm drug class

This medicine belongs to the Other ectoparasiticides, incl. scabicides class.

Drug family (ATC) Other ectoparasiticides, incl. scabicides
Where does this data come from?
Therapeutic classes from RxNorm RxClass (U.S. National Library of Medicine) — Established Pharmacologic Class (FDA), ATC drug family (WHO) and mechanism of action, matched by this product’s RxCUI.

Clinical

🧪 What is this product?

This is an over-the-counter moisturizing lotion containing dimethicone, a silicone-based ingredient. Applied directly to the skin, dimethicone is commonly used as an emollient and skin protectant that helps form a protective barrier and soften dry skin. This product is marketed under FDA's over-the-counter monograph rules for skin care products in this category.

Supplement & herbal interactions

Some supplements/herbs that may interact with Dimethicone — tap one for details:

Dimethylsulfoxide (dmso)Moderate Turpentine OilModerate AlchemillaMinor
🌿 Every supplement checked against Dimethicone (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: 2 bottles 532 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
11673-0087-18 You're viewing this Main listing 85 mL in 1 TUBE 2009-05-01 — Active
11673-0087-43 11673-087-43 532 mL in 1 BOTTLE 2011-08-29 — Active
11673-0087-98 11673-087-98 2 BOTTLE in 1 PACKAGE / 532 mL in 1 BOTTLE 2009-05-01 — Active

Pack size FAQ

What quantity is in this package?
This package contains 85 mL — 85 ml in 1 tube.
How does this package differ from NDC 11673-0087-43?
Both are Target Up and Up Daily Moisturizing Dimethicone 12 mg/mL Lotion — the drug itself is identical. This page's package is the 85 mL one, while NDC 11673-0087-43 is the 532 ml package.
What NDC number is used to bill for this package of Target Up and Up Daily Moisturizing Dimethicone 12 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
Daily Moisturizer 1.2 g/100g 00363-5934-02 Walgreens 236 ml — — FDA listed —
Daily Moisturizer 1200 mg/100mL 00363-5990-18 Walgreen 511 ml — — FDA listed —
Skin Relief 1200 mg/100mL 00363-5995-18 Walgreen 511 ml — — FDA listed —
Target Up and Up Daily Moisturizing 12 mg/mLthis 11673-0087-18 TARGET 85 ml — — FDA listed —
Dimethicone 12 mg/g 37808-0496-34 H 227 g — — FDA listed —
Hill Country Essentials 12 mg/mL 37808-0995-43 H.E.B 532 ml — — FDA listed —
Meijer Skin Relieving Moisturizing 12 mg/mL 41250-0985-43 MEIJER 532 ml — — FDA listed —
Equate Daily Moisturizing Dimethicone Skin Protectant 12 mg/mL 49035-0575-43 Walmart 532 ml — — FDA listed —
Baby XtraCare Oatmeal 1.2 g/100g 57337-0070-01 Rejoice 227 g — — FDA listed —
Alike Daily Moisturizing 1.2 g/100mL 57337-0098-01 Rejoice 354 ml — — FDA listed —
Life is healed Daily Moisturizing 12 mg/mL 63148-0028-05 Apollo 532 ml — — FDA listed —
Daily Moisturizing 12 mg/g 64024-0496-34 Aldi, 227 g — — FDA listed —
Aveeno Skin Relief Moisturizing Fragrance Free 12 mg/mL 69968-0236-09 Kenvue 975 ml — — FDA listed —
Aveeno Skin Relief Moisturizing Fragrance Free 12 mg/mL 69968-0408-01 Kenvue 29 ml — — FDA listed —
Aveeno Skin Relief Moisturizing Fragrance Free 12 mg/g 69968-0409-01 Kenvue 227 g — — FDA listed —
Aveeno Baby Daily Moisture 12 mg/mL 69968-0441-01 Kenvue 532 ml — — FDA listed —
Aveeno DAILY MOISTURIZING 12 mg/mL 69968-0454-01 Kenvue 354 ml — — FDA listed —
Aveeno Baby Daily Care Set 69968-0592-01 Kenvue 1 kit — — FDA listed —
Aveeno Baby Calming Comfort 12 mg/mL 69968-0629-01 Kenvue 532 ml — — FDA listed —
Aveeno Baby Calming Comfort Bath Plus Set 69968-0631-09 Kenvue 1 kit — — FDA listed —
Aveeno Baby Daily Care Set 69968-0632-09 Kenvue 1 kit — — FDA listed —
Aveeno Baby Calming Comfort 12 mg/g 69968-0656-08 Kenvue 227 g — — FDA listed —
Aveeno Baby Daily Moisture 12 mg/g 69968-0679-08 Kenvue 227 g — — FDA listed —
Aveeno Daily Moisturizing 12 mg/g 69968-0680-04 Kenvue 71 g — — FDA listed —
Daily Moisturizing 12 mg/g 71141-0496-34 Lidl 227 g — — FDA listed —
Daily Moisturizing 12 mg/g 75712-0496-34 Old 227 g — — Discontinued —
Dimethicone 12 mg/mL 76162-0496-44 Topco 532 ml — — FDA listed —
Dimethicone 12 mg/mL 79481-0496-01 Meijer, 532 ml — — FDA listed —
Aveeno Baby Daily Moisture with Coconut Oil and Shea Butter 12 mg/mL 69968-0762-01 Kenvue 354 ml — — 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

🏛️
2009
On the market since
May 2009
📍
2026
Currently FDA-listed
17 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.

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 X7GNG3S47T
    A quaternary ammonium compound used as an antistatic agent and emulsifier in pharmaceutical formulations. It helps reduce static electricity during manufacturing and improves texture or consistency in creams and lotions.
  • UNII LKG8494WBH
    Benzyl alcohol is a clear liquid used as a preservative and solvent in medicines. It helps prevent bacterial and fungal growth and dissolves other ingredients to create uniform liquid formulations.
  • UNII 2DMT128M1S
    A waxy solid derived from plant or animal sources. It acts as an emulsifier to blend oil and water components, and also thickens the medicine to give it the right texture and consistency.
  • UNII 936JST6JCN
    Cetyl alcohol is a waxy, fatty substance derived from plant or animal sources. It acts as an emulsifier and thickener in medicines, helping blend oil and water components and giving products a smooth, creamy texture.
  • 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 8CRQ2TH63M
    Isopropyl palmitate is an oily liquid derived from palm oil. It acts as an emollient and lubricant in medicines, helping soften the skin or improve how the product spreads and flows.
  • UNII 8PI54V663Y
    Oatmeal is ground oat grain used as a natural filler and texture agent in medicines. It absorbs moisture, adds bulk to the formulation, and may help create a soothing base in topical products.
  • UNII 4T6H12BN9U
    Petrolatum is a purified mineral oil-based jelly derived from petroleum. In medicines, it acts as an emollient, lubricant, and moisture barrier to soften skin, reduce friction, and help prevent water loss from formulations.
  • UNII 67C1D6YV24
    Polyquaternium 37 is a synthetic polymer used as a thickening agent and viscosity enhancer in liquid medications and topical products. It increases the consistency of formulations to improve texture and help active ingredients spread evenly.
  • 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 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.

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

The official label also statesavena sativa (oat) kernel flour, behenrimonium chloride, benzyl alcohol, cetearyl alcohol, cetyl alcohol, glycerin, isopropyl palmitate, petrolatum, polyquaterium-37, sodium chloride, water.

Label-section wording can be broader than the structured product block and may mention additional formulation ingredients.

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

LabelerTARGET CORPORATION
FDA applicationM016 (OTC MONOGRAPH DRUG)
Labeler code11673
First marketedMay 2009
Product typeHuman Otc Drug
Portfolio409 products on file
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 📄 Do Not Use 📄 Ask a Doctor Before Use If 📄 When Using This Product 📄 Keep Out of Reach of Children 📄 Other Information 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 30 words ▾

Uses helps prevent sunburn if used as directed with other sun protection measures (see Directions ), decreases the risk of skin cancer and early skin aging caused by the sun

⏱️ Dosage and Administration 14 words ▾

Directions apply as needed to hands or body when skin feels dry or irritated

⚠️ Warnings 5 words ▾

Warnings For external use only

🧪 Active Ingredient 4 words ▾

Active ingredients Dimethicone 1.2%

🧪 Inactive Ingredients 23 words ▾

Inactive ingredients avena sativa (oat) kernel flour, behenrimonium chloride, benzyl alcohol, cetearyl alcohol, cetyl alcohol, glycerin, isopropyl palmitate, petrolatum, polyquaterium-37, sodium chloride, water.

🎯 Purpose 3 words ▾

Purpose Skin Protectant

📄 Do Not Use 14 words ▾

When using this product • keep out of eyes. Rinse with water to remove.

📄 Ask a Doctor Before Use If 27 words ▾

Stop use and ask a doctor if • condition worsens • symptoms last more than seven days or clear up and occur again within a few days

📄 When Using This Product 14 words ▾

Do not use • deep or puncture wounds • animal bites • serious burns

📄 Keep Out of Reach of Children 19 words ▾

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

📄 Other Information 6 words ▾

Other information may stain some fabrics

📄 Package Label / Principal Display Panel 2 words ▾

Label 82845E8F9

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

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 — Not published for this NDC No photo available yet for this listing.
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 TARGET CORPORATION. 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 2 other package presentations of this same product, including 2 bottles (11673-0087-98), 532 ml (11673-0087-43). 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?
TARGET CORPORATION 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.
← 11673-0079-00 · Target 11673-0088-17 · TARGET →
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.