Label: HAND-AID- alcohol gel
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NDC Code(s):
62257-122-01,
62257-122-13,
62257-122-14,
62257-122-17, view more62257-122-21, 62257-122-24, 62257-122-28, 62257-122-47, 62257-122-55
- Packager: ABC Compounding Co., Inc.
- 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 January 15, 2021
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- Drug Facts Box OTC-Active Ingredient Section
- Drug Facts Box OTC-Purpose Section
- Drug Facts Box OTC-Indications & Usage Section
- Drug Facts Box OTC-Warnings Section
- Drug Facts Box OTC-When Using Section
- Drug Facts Box OTC-Stop Use Section
- Drug Facts Box OTC-Keep Out of Reach of Children Section
- Drug Facts Box OTC-Dosage & Administration Section
- Drug Facts Box OTC-Inactive Ingredient Section
- Hand-Aid 6605 Drug Facts and Label
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INGREDIENTS AND APPEARANCE
HAND-AID
alcohol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:62257-122 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 0.7 mL in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) CARBOMER 934 (UNII: Z135WT9208) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) ALOE VERA LEAF (UNII: ZY81Z83H0X) .ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8) DIISOPROPYLAMINE (UNII: BR9JLI40NO) DMDM HYDANTOIN (UNII: BYR0546TOW) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:62257-122-17 532 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 01/15/2021 2 NDC:62257-122-24 118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 01/15/2021 3 NDC:62257-122-01 1200 mL in 1 CARTRIDGE; Type 0: Not a Combination Product 01/15/2021 4 NDC:62257-122-28 149 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 01/15/2021 5 NDC:62257-122-14 3785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 01/15/2021 6 NDC:62257-122-13 800 mL in 1 BAG; Type 0: Not a Combination Product 01/15/2021 7 NDC:62257-122-47 473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 01/15/2021 8 NDC:62257-122-17 532 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 01/15/2021 9 NDC:62257-122-55 208200 mL in 1 DRUM; Type 0: Not a Combination Product 01/15/2021 10 NDC:62257-122-21 2.5 mL in 1 DOSE PACK; Type 0: Not a Combination Product 01/15/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 01/15/2021 Labeler - ABC Compounding Co., Inc. (003284353) Registrant - ABC Compounding Co., Inc. (003284353) Establishment Name Address ID/FEI Business Operations ABC Compounding Co., Inc. 003284353 manufacture(62257-122)