Label: HAND RELIEF- lotion lotion
- NDC Code(s): 70741-012-03
- 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 August 18, 2023
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- ACTIVE INGREDIENT
- PURPOSE
- WARNINGS
- WHEN USING
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
- DOSAGE & ADMINISTRATION
- OTHER SAFETY INFORMATION
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INACTIVE INGREDIENT
Water (aqua), glycereth-18 (and) glycereth-18 ethylhexanoate, PEG 1450, PEG-10 dimethicone, ethylene glycol distearate, PEG 75 lanolin, cocamide MEA, retinyl palmitate (Vitamin A), magnesium ascorbyl phosphate (Vitamin C), d-l alpha tocopherol acetate (Vitamin E), acrylate crosspolymer, 2-amino-2-methyl-1-propanol, Cocos nucifera (Coconut oil), mentha piperita extract.
- SPL UNCLASSIFIED SECTION
- SPL UNCLASSIFIED SECTION
- QUESTIONS
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- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
HAND RELIEF
lotion lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70741-012 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) 25 mL in 100 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70741-012-03 120 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 08/08/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 08/08/2023 Labeler - Derma Glove (962709569) Registrant - Derma Glove (962709569) Establishment Name Address ID/FEI Business Operations RWM Technologies 626626969 manufacture(70741-012)