Label: BUDDLE DIAPER RASH RESCUE HEALING- white petrolatum, zinc oxide paste
- NDC Code(s): 83178-101-04
- Packager: The Goodsprout Company LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 7, 2023
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- Active Ingredients
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Inactive Ingredients
anhydrous lanolin, polyglyceryl-2 dipolyhydroxystearate, zea mays (corn) starch, beeswax white, ceramide AP, ceramide NP, ceramide EOP, honey, water, alpha-glucan oligosaccharide, lactobacillus ferment, taraxacum officinale (dandelion) leaf extract, inulin, phytosphingosine, cetyI alcohol, butylene glycol, carbomer, xanthan gum, ethylhexylglycerin, 1,2-hexanediol, sodium lauroyl lactylate, cholesterol
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INGREDIENTS AND APPEARANCE
BUDDLE DIAPER RASH RESCUE HEALING
white petrolatum, zinc oxide pasteProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:83178-101 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength WHITE PETROLATUM (UNII: B6E5W8RQJ4) (WHITE PETROLATUM - UNII:B6E5W8RQJ4) WHITE PETROLATUM 50.7 g in 100 g ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 40 g in 100 g Inactive Ingredients Ingredient Name Strength HONEY (UNII: Y9H1V576FH) WATER (UNII: 059QF0KO0R) CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) WHITE WAX (UNII: 7G1J5DA97F) CERAMIDE NP (UNII: 4370DF050B) POLYGLYCERYL-2 DIPOLYHYDROXYSTEARATE (UNII: 9229XJ4V12) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) STARCH, CORN (UNII: O8232NY3SJ) INULIN (UNII: JOS53KRJ01) TARAXACUM OFFICINALE LEAF (UNII: 0022LFJ74Y) .ALPHA.-GLUCAN OLIGOSACCHARIDE (UNII: S95658MI3W) CHOLESTEROL (UNII: 97C5T2UQ7J) 1,2-HEXANEDIOL (UNII: TR046Y3K1G) CERAMIDE AP (UNII: F1X8L2B00J) PHYTOSPHINGOSINE (UNII: GIN46U9Q2Q) LIMOSILACTOBACILLUS FERMENTUM (UNII: 2C1F12C6AP) SODIUM LAUROYL LACTYLATE (UNII: 7243K85WFO) CERAMIDE 1 (UNII: 5THT33P7X7) LANOLIN (UNII: 7EV65EAW6H) CETYL ALCOHOL (UNII: 936JST6JCN) XANTHAN GUM (UNII: TTV12P4NEE) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:83178-101-04 113 g in 1 TUBE; Type 0: Not a Combination Product 12/01/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M016 12/01/2023 Labeler - The Goodsprout Company LLC (118309464)