BEBE BOTTOMS- zinc oxide spray 
TARO PHARMACEUTICALS U.S.A., INC.

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Bebe Bottoms™

Drug Facts

Active ingredient

Zinc oxide 10%

Purpose

Skin protectant

Uses

Warnings

For external use only

When using this product

  • do not get into eyes

Stop use and contact a doctor if

  • condition worsens
  • symptoms last more than 7 days or clear up and reoccur within a few days
  • not to be applied over deep or puncture wounds, infection or lacerations

Keep out of reach of children

  • If swallowed, get medical help or contact a Poison Control Center right away (1-800-222-1222).

Directions

Other information

Store at room temperature, below 77°F.

Inactive ingredients

alkyl-alcohols, alkyl glucoside, calendula officinalis flower extract, caprylyl glycol, caprylhydroxamic acid, chamomilla recutita (matricaria) flower extract, coco-caprylate/caprate, cocoglycerides, glycerin, oleic acid, potassium sorbate, propylene glycol, silica, sodium benzoate, water

Questions?

call 1-866-923-4914

Distributed by: Taro Pharmaceuticals U.S.A., Inc.,
Hawthorne, NY 10532 PRODUCT OF NETHERLANDS

PRINCIPAL DISPLAY PANEL - 100 mL Bottle Carton

bébé
BOTTOMS

DIAPER RASH
CRÈME SPRAY

10% ZINC OXIDE
SKIN PROTECTANT

PREVENTS & TREATS
FOR DAILY USE

NET WT. 3.4 OZ (100 mL)

PRINCIPAL DISPLAY PANEL - 100 mL Bottle Carton
BEBE BOTTOMS 
zinc oxide spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:51672-5318
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE100 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
C14-22 ALCOHOLS (UNII: B1K89384RJ)  
C12-20 ALKYL GLUCOSIDE (UNII: K67N5Z1RUA)  
CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)  
caprylyl glycol (UNII: 00YIU5438U)  
caprylhydroxamic acid (UNII: UPY805K99W)  
CHAMOMILE (UNII: FGL3685T2X)  
COCOYL CAPRYLOCAPRATE (UNII: 8D9H4QU99H)  
COCO-GLYCERIDES (UNII: ISE9I7DNUG)  
glycerin (UNII: PDC6A3C0OX)  
oleic acid (UNII: 2UMI9U37CP)  
potassium sorbate (UNII: 1VPU26JZZ4)  
propylene glycol (UNII: 6DC9Q167V3)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
sodium benzoate (UNII: OJ245FE5EU)  
water (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:51672-5318-31 in 1 CARTON12/01/2023
150 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product
2NDC:51672-5318-71 in 1 CARTON12/01/2023
2100 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph drugM01612/01/2023
Labeler - TARO PHARMACEUTICALS U.S.A., INC. (145186370)

Revised: 11/2023
Document Id: b3f54a92-14fb-438e-8c48-b33706e5d719
Set id: eb8512db-f8a9-432c-8779-2971411ce43d
Version: 3
Effective Time: 20231121
 
TARO PHARMACEUTICALS U.S.A., INC.