Label: SHELO NABEL CREMA BABA DE CARACOL- allantoin cream
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Contains inactivated NDC Code(s)
NDC Code(s): 71424-1001-1 - Packager: Corporativo Serysi S de R L de C V
- 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 October 15, 2019
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- Active Ingredient U001
- Inactive Ingredient U001
- Warnings U001
- Purpose U001
- KOROC U001
- Administration
- INdications U001
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INGREDIENTS AND APPEARANCE
SHELO NABEL CREMA BABA DE CARACOL
allantoin creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71424-1001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z) ALLANTOIN 10 mg in 1 g Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71424-1001-1 300 g in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product 05/19/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part347 05/19/2017 Labeler - Corporativo Serysi S de R L de C V (816628390) Registrant - Corporativo Serysi S de R L de C V (816628390)
