Label: SHELO NABEL D B T CREAM- allantoin cream
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Contains inactivated NDC Code(s)
NDC Code(s): 71424-1145-1 - 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
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient U145
- Inactive Ingredient U145
- Warnings U145
- Purpose U145
- KOROC
- Administration U145
- Indcations U145
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INGREDIENTS AND APPEARANCE
SHELO NABEL D B T CREAM
allantoin creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71424-1145 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z) ALLANTOIN 5 mg in 1 g Inactive Ingredients Ingredient Name Strength ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M) Product Characteristics Color white Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71424-1145-1 280 g in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product 05/18/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part347 05/18/2017 Labeler - Corporativo Serysi S de R L de C V (816628390) Registrant - Corporativo Serysi S de R L de C V (816628390)
