Label: HAND- lotion lotion
- NDC Code(s): 70741-006-03
- Packager: Derma Glove
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not 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 May 8, 2020
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- WARNINGS
- WHEN USING
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
- DOSAGE & ADMINISTRATION
- OTHER SAFETY INFORMATION
- INACTIVE INGREDIENT
- QUESTIONS
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
HAND
lotion lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70741-006 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Alcohol (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) Alcohol 70 mL in 100 mL Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) 20 mL in 100 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70741-006-03 75 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 09/14/2016 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 08/31/2016 Labeler - Derma Glove (962709569) Registrant - Derma Glove (962709569) Establishment Name Address ID/FEI Business Operations RWM Technologies Inc. 626626969 manufacture(70741-006)