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Aveeno Baby Daily Care Set Dimethicone Kit — NDC 69968-0632-09 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Aveeno Baby Daily Care Set Dimethicone Kit — NDC 69968-0632-9 (Billing 69968-0632-09)

by Kenvue Brands LLC · 1 KIT in 1 PACKAGE * 354 mL in 1 BOTTLE, PUMP * 354 mL in 1 BOTTLE, PUMP

This is a package of Aveeno Baby Daily Care Set Dimethicone Kit from Kenvue Brands LLC, marketed since Nov 2020 and currently FDA-listed. It is this product's only package size.

NDC 69968-0632-09
🏷️ FDA NDC (as labeled) 69968-0632-9 billing pads the package segment with a zero
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 69968-0632-9 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
69968 labeler · 0632 product · 9 package
Package marketed since
Nov 30, 2020
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Barcode (UPC-A, from the NDC)
3 6996806329 9
FDA record last changed
Jul 24, 2026
⚠️
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) 69968-0632-9
Product NDC 69968-0632
11-digit billing NDC 69968063209
RxCUI 876980
Application # M016
SPL Set ID 3d3da49e-dba6-4c6b-9278-5c8692e29f14
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2020-11-30
Dosage form KIT
Quick answers
  • RxCUI (RxNorm): 876980
Why two NDCs? The FDA registers this code as 69968-0632-9 — a 5-4-1 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 package segment → 69968-0632-09. 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 baby care kit containing dimethicone, a skin protectant that is commonly used to create a moisture barrier on the skin. Dimethicone is typically included in baby products to help soothe and protect delicate skin from irritation and moisture loss. The kit format allows caregivers to use the product as directed on individual components for routine baby skin care.

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 eachPer 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.
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
69968-0632-09 You're viewing this Main listing 1 KIT in 1 PACKAGE * 354 mL in 1 BOTTLE, PUMP * 354 mL in 1 BOTTLE, PUMP 2020-11-30 — Active

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/mL 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 Setthis 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 Welcome Little One Gift Basket 69968-0766-09 Kenvue 1 kit — — 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

🏛️
2020
On the market since
Nov 2020
📍
2026
Currently FDA-listed
6 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.

From the label’s inactive-ingredient sectionWater, Glycerin, Distearyldimonium Chloride, Petrolatum, Isopropyl Palmitate, Cetyl Alcohol, Avena Sativa (Oat) Kernel Flour, Benzyl Alcohol, Sodium Chloride, Allantoin

This is label-wide narrative text, not a normalized exact-product ingredient list. A label can cover multiple strengths or packages.

Where does this data come from?
Source: official FDA Structured Product Labeling (SPL) via DailyMed and the openFDA label index. Structured IACT rows and label-wide narrative are kept separate; availability and product-level specificity depend on the submitted label.

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

LabelerKenvue Brands LLC
FDA applicationM016 (OTC MONOGRAPH DRUG)
Labeler code69968
First marketedNov 2020
Product typeHuman Otc Drug
Portfolio567 products on file

More NDCs from Kenvue Brands LLC labeler code 69968

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 📦 Storage and Handling 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose 📄 Do Not Use 📄 When Using This Product 📄 Stop Use and Ask a Doctor If 📄 Keep Out of Reach of Children 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 11 words ▾

Uses Helps prevent and temporarily protects chafed, chapped or cracked skin.

⏱️ Dosage and Administration 4 words ▾

Directions Apply as needed.

⚠️ Warnings 70 words ▾

Warnings For external use only When using this product Do not get into eyes Stop use and ask a doctor if Condition worsens Symptoms last more than 7 days or clear up and occur again within a few days Do not use on Deep or puncture wounds Animal bites Serious burns Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

📦 Storage and Handling 17 words ▾

Other information Remove quality seal. Do not use if quality seal is broken. Store at room temperature.

🧪 Active Ingredient 4 words ▾

Active ingredient Dimethicone 1.2%

🧪 Inactive Ingredients 21 words ▾

Inactive ingredients Water, Glycerin, Distearyldimonium Chloride, Petrolatum, Isopropyl Palmitate, Cetyl Alcohol, Avena Sativa (Oat) Kernel Flour, Benzyl Alcohol, Sodium Chloride, Allantoin

🎯 Purpose 3 words ▾

Purpose Skin protectant

📄 Do Not Use 12 words ▾

Do not use on Deep or puncture wounds Animal bites Serious burns

📄 When Using This Product 9 words ▾

When using this product Do not get into eyes

📄 Stop Use and Ask a Doctor If 25 words ▾

Stop use and ask a doctor if Condition worsens Symptoms last more than 7 days or clear up and occur again within a few days

📄 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.

📄 Questions or Comments 8 words ▾

Questions? 866-428-3366; Outside US, dial collect 215-273-8755 www.aveeno.com

📄 Package Label / Principal Display Panel 44 words ▾

PRINCIPAL DISPLAY PANEL - Kit Package Label RECOMMENDED BY PEDIATRICIANS & DERMATOLOGISTS Aveeno ® baby daily care set daily nourishment for baby's sensitive skin cleanse gently protect and moisturize 12 FL OZ (354mL) 12 FL OZ (354mL) PRINCIPAL DISPLAY PANEL - Kit Package Label

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 Aveeno Baby Daily Care Set (this brand).

Top reported reactions

Vomiting56
Diarrhoea52
Abdominal Pain49
Pyrexia48
Nausea47
Pneumonia41
Decreased Appetite35

Reporter sex

676 reports
Male · 49%
Female · 51%
Unknown · 0%

Serious outcomes

Death131
Life-threatening60
Reports over time (by year) — tap or hover for the count & year
2019 2021 2023 2026 114 28
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 Kit / multi-component package

Kit / multi-component package

This NDC identifies a kit — a package containing more than one component. Structured data (pricing, ingredients, equivalents) is often reported per component rather than for the kit NDC itself, which can make this page look thinner than the components' own pages.

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 Kenvue Brands LLC. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Kenvue Brands LLC 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.
← 69968-0631-09 · Kenvue 69968-0633-09 · Kenvue →
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.