Label: ALCO SAN- alcohol gel
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NDC Code(s):
64233-221-01,
64233-221-03,
64233-221-05,
64233-221-06, view more64233-221-07, 64233-221-08, 64233-221-09, 64233-221-10, 64233-221-11, 64233-221-12, 64233-221-13, 64233-221-14, 64233-221-15, 64233-221-17, 64233-221-24, 64233-221-27, 64233-221-28, 64233-221-55
- Packager: Mid American Research Chemical Corp
- 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 2, 2019
If you are a consumer or patient please visit this version.
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- 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
- Alco San 6605 5oz
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INGREDIENTS AND APPEARANCE
ALCO SAN
alcohol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:64233-221 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:64233-221-06 1 in 1 BOX 07/01/2015 1 800 mL in 1 BAG; Type 0: Not a Combination Product 2 NDC:64233-221-17 532 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 07/01/2015 3 NDC:64233-221-24 118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 07/01/2015 4 NDC:64233-221-01 1200 mL in 1 CARTRIDGE; Type 0: Not a Combination Product 07/01/2015 5 NDC:64233-221-03 350 mL in 1 CARTRIDGE; Type 0: Not a Combination Product 07/01/2015 6 NDC:64233-221-05 540 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 07/01/2015 7 NDC:64233-221-07 700 mL in 1 BAG; Type 0: Not a Combination Product 07/01/2015 8 NDC:64233-221-09 2000 mL in 1 CARTRIDGE; Type 0: Not a Combination Product 07/01/2015 9 NDC:64233-221-10 1000 mL in 1 CARTRIDGE; Type 0: Not a Combination Product 07/01/2015 10 NDC:64233-221-11 1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 07/01/2015 11 NDC:64233-221-12 1000 mL in 1 BAG; Type 0: Not a Combination Product 07/01/2015 12 NDC:64233-221-13 800 mL in 1 BAG; Type 0: Not a Combination Product 07/01/2015 13 NDC:64233-221-14 3785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 07/01/2015 14 NDC:64233-221-15 946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 07/01/2015 15 NDC:64233-221-28 149 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 07/01/2015 16 NDC:64233-221-27 800 mL in 1 CARTRIDGE; Type 0: Not a Combination Product 07/01/2015 17 NDC:64233-221-55 208200 mL in 1 DRUM; Type 0: Not a Combination Product 07/01/2015 18 NDC:64233-221-08 1 in 1 BOX 07/01/2015 18 1000 mL in 1 BAG; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 07/01/2015 Labeler - Mid American Research Chemical Corp (051254092) Registrant - ABC Compounding Co., Inc. (003284353) Establishment Name Address ID/FEI Business Operations ABC Compounding Co., Inc. 003284353 manufacture(64233-221)