Label: ATO ALL- glycerin liquid
-
Contains inactivated NDC Code(s)
NDC Code(s): 69224-1001-1 - Packager: GL BioTech
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph 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 October 17, 2014
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- INACTIVE INGREDIENT
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
-
INDICATIONS & USAGE
1. For the first 5 days, spray 3 times a day for
breakfast, lunch and dinner
2. After shower dry your body completely and
then spray.
3. Spraying on the trouble spot may hurt due to
disinfecting action.
4. Please refrain from the food that
accompanies a skin reaction.
5. After use, you might want to use the other
basic cosmetic products.
- WARNINGS
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
ATO ALL
glycerin liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69224-1001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) GLYCERIN 2 g in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ALCOHOL (UNII: 3K9958V90M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69224-1001-1 100 mL in 1 BOTTLE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part347 10/17/2014 Labeler - GL BioTech (689057539) Registrant - GL BioTech (689057539) Establishment Name Address ID/FEI Business Operations GL BioTech 689057539 manufacture(69224-1001)