![FREE HAND (ALCOHOL) GEL [ATCO INTERNATIONAL]](https://medic.hrt.org//dailymed/images/a03d1e0c-3bd1-4f6e-af37-c649a20b225f/660518S77.jpg)
- 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
- Free Hand 6605 18oz
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INGREDIENTS AND APPEARANCE
FREE HAND
alcohol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:62712-221 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) DMDM HYDANTOIN (UNII: BYR0546TOW) ALOE VERA LEAF (UNII: ZY81Z83H0X) .ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8) DIISOPROPYLAMINE (UNII: BR9JLI40NO) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:62712-221-17 532 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 10/01/2009 2 NDC:62712-221-24 118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 10/01/2009 3 NDC:62712-221-28 149 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 10/01/2009 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 10/01/2009 Labeler - Atco International (033504929) Registrant - ABC Compounding Co., Inc. (003284353) Establishment Name Address ID/FEI Business Operations ABC Compounding Co., Inc. 003284353 manufacture(62712-221)
