Label: BLACKBERRY VANILLA HAND SANITIZER BODYCOLOGY- alcohol liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 49035-107-01, 49035-107-02 - Packager: Wal-Mart Stores 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 May 21, 2013
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
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ACTIVE INGREDIENT
Active ingredient Purpose
Alcohol 75% Antiseptic
Uses To decrease bacteria on the skin.
Keep out of reach of children. In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.
Discontinue use if irritation and redness develop. If condition persists for more than 72 hours, consult a doctor.
Warnings
For external use only.
FLAMMABLE. Keep away from flame or high heat.
When using this product
Avoid contact with eyes. If contact occurs, flush eyes with water.
Avoid contact with broken skin
Directions
Wet hands thoroughly with product and allow to dry without wiping.
For children under 6, use only under adult supervision.
Not recommended for infants.
Inactive ingredients: Water (Aqua, Eau), Fragrance (Parfum), Propylene Glycol, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Triethanolamine, Gelatin, Tocopheryl Acetate, Aloe Barbadensis Leaf Juice, Ultramarines (CI 77007).
May Contain: FD&C Red No. 4 (CI 14700), FD&C Yellow No. 5 (CI 19140), FD&C Blue No. 1 (CI 42090), D&C Red No. 33 (CI 17200).
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
BLACKBERRY VANILLA HAND SANITIZER BODYCOLOGY
alcohol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49035-107 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 75 g in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 71DD5V995L) TROLAMINE (UNII: 9O3K93S3TK) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) GELATIN (UNII: 2G86QN327L) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) ALOE VERA LEAF (UNII: ZY81Z83H0X) ULTRAMARINE BLUE (UNII: I39WR998BI) FD&C RED NO. 4 (UNII: X3W0AM1JLX) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) D&C RED NO. 33 (UNII: 9DBA0SBB0L) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49035-107-02 1 in 1 PACKAGE 1 NDC:49035-107-01 30 mL in 1 BOTTLE, PLASTIC Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 05/21/2013 Labeler - Wal-Mart Stores Inc (051957769) Registrant - Wal-Mart Stores Inc (051957769) Establishment Name Address ID/FEI Business Operations Landy International 545291775 manufacture(49035-107)
