Label: HYDRA C3 TRIPLE RESET- witch hazel cream
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Contains inactivated NDC Code(s)
NDC Code(s): 71276-100-01, 71276-100-02 - Packager: ULAB
- 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 March 22, 2017
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- ACTIVE INGREDIENT
- INACTIVE INGREDIENT
- PURPOSE
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
- DOSAGE & ADMINISTRATION
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
HYDRA C3 TRIPLE RESET
witch hazel creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71276-100 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength WITCH HAZEL (UNII: 101I4J0U34) (WITCH HAZEL - UNII:101I4J0U34) WITCH HAZEL 3.0 g in 60 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Glycerin (UNII: PDC6A3C0OX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71276-100-02 1 in 1 CARTON 03/02/2017 1 NDC:71276-100-01 60 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part347 03/02/2017 Labeler - ULAB (688976692) Registrant - ULAB (688976692) Establishment Name Address ID/FEI Business Operations ULAB 688976692 relabel(71276-100) Establishment Name Address ID/FEI Business Operations U-LAB Switzerland AG 485958743 manufacture(71276-100)