Label: BODY BLENDS VANILLA SUGAR ANTI-BACTERIAL HAND SANITIZER- alcohol liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 49981-021-01 - Packager: Xiamen Anna Global Co., Ltd
- Category: HUMAN OTC DRUG LABEL
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 July 5, 2010
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- ACTIVE INGREDIENT
- DESCRIPTION
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WARNINGS
Warnings
For external use only
Flammable: Keep away from fire or flame
When using this product,avoid contact with eyes. If contact occurs, flush with water
Stop using and ask a doctor, if irritation or rash persists
Keep out of reach of children and pets. If swallowed, get medical help or contact a Poison Control Center immediately.
- WHEN USING
- INACTIVE INGREDIENT
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
BODY BLENDS VANILLA SUGAR ANTI-BACTERIAL HAND SANITIZER
alcohol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49981-021 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 62.00 g in 100 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) 34.04989 g in 100 g PROPYLENE GLYCOL (UNII: 6DC9Q167V3) 1.8 g in 100 g POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F) 1.0 g in 100 g CARBOMER COPOLYMER TYPE A (UNII: 71DD5V995L) 0.29 g in 100 g TROLAMINE (UNII: 9O3K93S3TK) 0.28 g in 100 g ANHYDROUS LACTOSE (UNII: 3SY5LH9PMK) 0.01 g in 100 g CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U) 0.01 g in 100 g EDETATE DISODIUM (UNII: 7FLD91C86K) 0.03 g in 100 g FD&C RED NO. 4 (UNII: X3W0AM1JLX) 0.00003 g in 100 g FD&C YELLOW NO. 5 (UNII: I753WB2F1M) 0.00008 g in 100 g HYPROMELLOSE 2208 (15000 CPS) (UNII: Z78RG6M2N2) 0.01 g in 100 g ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) 0.01 g in 100 g ASCORBYL PALMITATE (UNII: QN83US2B0N) 0.01 g in 100 g VANILLA (UNII: Q74T35078H) 0.5 g in 100 g Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49981-021-01 59 g in 1 BOTTLE, PLASTIC Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333 07/10/2010 Labeler - Xiamen Anna Global Co., Ltd (527060704) Registrant - Xiamen Anna Global Co., Ltd (527060704) Establishment Name Address ID/FEI Business Operations Xiamen Anna Global Co., Ltd 527060704 manufacture