Label: DAILY BABY- dimethicone lotion
- NDC Code(s): 0363-2247-34
- Packager: WALGREEN CO
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated July 26, 2023
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- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Uses
- Warnings
- Do not use on
- When using this product
- Stop use and ask a doctor if
- Keep out of reach of children.
- Directions
- Other information
- Inactive ingredients
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SPL UNCLASSIFIED SECTION
†Our pharmacists recommend the Walgreens brand. We invite you to compare to national brands.
††This product is not manufactured or distributed by Johnson & Johnson, owner of the registered trademark Aveeno Baby®.
DISTRIBUTED BY: Walgreen Co.
200 Wilmot Rd., Deerfield, IL 60015
Walgreens 100% Satisfaction Guaranteed
walgreens.com 1-800-925-4733
©2021 Walgreen Co.
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PRINCIPAL DISPLAY PANEL
Walgreens
WALGREENS PHARMACIST RECOMMENDED†
Compare to the active ingredient in Aveeno Baby® Daily Moisture Lotion®††
Baby Lotion
with Colloidal Oatmeal
Dimethicone 1.2%/Skin Protectant
Non-greasy
Hypoallergenic
- Fragrance, paraben, phthalate & quaternium-15 free
- Helps heal & protect baby's skin
- Pediatrician & allergy tested
Net Wt 8 oz (227 g)
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INGREDIENTS AND APPEARANCE
DAILY BABY
dimethicone lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0363-2247 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DIMETHICONE (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O) DIMETHICONE 12 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) DISTEARYLDIMONIUM CHLORIDE (UNII: OM9573ZX3X) PETROLATUM (UNII: 4T6H12BN9U) ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M) CETYL ALCOHOL (UNII: 936JST6JCN) OATMEAL (UNII: 8PI54V663Y) BENZYL ALCOHOL (UNII: LKG8494WBH) SODIUM CHLORIDE (UNII: 451W47IQ8X) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0363-2247-34 227 mL in 1 TUBE; Type 0: Not a Combination Product 11/13/2018 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part347 11/13/2018 Labeler - WALGREEN CO (008965063) Registrant - Vi-Jon (790752542) Establishment Name Address ID/FEI Business Operations Vi-Jon 790752542 manufacture(0363-2247) Establishment Name Address ID/FEI Business Operations Vi-Jon 088520668 manufacture(0363-2247)