Label: BABY OILOGIC SKIN AID DIAPER RASH- zinc oxide spray
- NDC Code(s): 79948-057-00
- Packager: Ignite Brands, LLC
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated June 7, 2024
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Drug Facts
- Active ingredient
- Use(s)
- Warnings
- Directions
-
Inactive Ingredients:
Acacia Senegal Gum, Calendula Officinalis Flower Extract, Caprylhydroxamic Acid, Caprylic/Capric Triglyceride, Caprylyl Glycol, Cellulose Gum, Coco-Caprylate/Caprate, Cocos Nucifera (Coconut) Oil, Glycerin, Lavandula Angustifolia (Lavender) Oil, Methyl Dihydroabietate, Microcrystalline Cellulose, Propanediol, Simmondsia Chinensis (Jojoba) Seed Oil, Tricaprylin, Water (Aqua), Xanthan Gum, Zinc Carbonate.
- Other Information
- Questions?
- package Labeling:
-
INGREDIENTS AND APPEARANCE
BABY OILOGIC SKIN AID DIAPER RASH
zinc oxide sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:79948-057 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION 150 mg in 1 mL Inactive Ingredients Ingredient Name Strength ACACIA (UNII: 5C5403N26O) CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD) CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) CAPRYLYL GLYCOL (UNII: 00YIU5438U) CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED (UNII: K679OBS311) COCO-CAPRYLATE/CAPRATE (UNII: 8D9H4QU99H) COCONUT OIL (UNII: Q9L0O73W7L) GLYCERIN (UNII: PDC6A3C0OX) LAVENDER OIL (UNII: ZBP1YXW0H8) METHYL DIHYDROABIETATE (UNII: 7666FJ0J9F) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) PROPANEDIOL (UNII: 5965N8W85T) JOJOBA OIL (UNII: 724GKU717M) TRICAPRILIN (UNII: 6P92858988) WATER (UNII: 059QF0KO0R) XANTHAN GUM (UNII: TTV12P4NEE) ZINC CARBONATE (UNII: EQR32Y7H0M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:79948-057-00 1 in 1 CARTON 06/01/2024 1 50.3 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M016 06/01/2024 Labeler - Ignite Brands, LLC (079843577)