Label: ABOVE WOMEN DERMA CLINICAL 72 H cream
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Contains inactivated NDC Code(s)
NDC Code(s): 73306-1138-1 - Packager: BASTON INDUSTRIA DE AEROSSOIS LTDA
- 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 November 14, 2022
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ALUMINUM CHLOROHYDRATE 12 %
- ROLL ON DEODORANT ANTIPERSPIRANT
- REDUCES UNDEARMS WETNESS
- AQUA CAPRYLIC/CAPRIC TRIGLYCERIDE STEARETH 2 GLYCINE CALCIUM CHLORIDE STEARETH-21 PARFUM SILICA ACRYLATES COPOLYMER CETEARETH-20 2-METHYL 5-CYCLOHEXYLPENTANOL MORINGA OLEIFERA SEED OIL ACRYLATES / C10-30 ALKYL ACRYLATE CROSS POLYMER MALTODEXTRIN CITRIC ACID SODIUM GLUCONATE GOSSYPIUM HERBACEUM SEED OIL SODIUM LAURETH SULFATE BUTYROSPERMUM PARKII BUTTER MACADAMIA TERNIFOLIA SEED OIL COCOS NUCIFERA FRUIT EXTRACT CHAMOMILLA RECUTITA FLOWER EXTRACT ALOE BARBADENSIS LEAF EXTRACT CAMELLIA SINENSIS LEAF EXTRACT CINNAMOMUM ZEYLANICUM BARK EXTRACT ACORUS CALAMUS ROOT EXTRACT COMMIPHORA MYRRHA RESIN EXTRACT OLEA EUROPAEA FRUIT OIL ARGANIA SPINOSA KERNEL OIL LECITHIN POLYGLYCERYL-3 DIISOSTEARATE GLYCERIN GLYCERYL STEARATE SILVER GLICERYLCITRATE / LACTATE / LINOLEATE / OLEATE
- SAC@BASTON.COM.BR OR CALL (305) 677-5030
- FOR EXTERNAL USE ONLY. DO NOT USE ON BROKEN SKIN .ASK A DOCTOR BEFORE USE IF YOU HAVE KIDNEY DISEASE.STOP USE IF RASH OR IRRITATION OCCURS. KEEP OUT OF REACH OF CHILDREN IF SWALLOWED, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER RIGHT AWAY.
- KEEP OUT OF THE CHILDREN
- USE ONLY UNDERARMS
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
ABOVE WOMEN DERMA CLINICAL 72 H
above women derma clinical 72 h creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73306-1138 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (ALUMINUM CHLOROHYDRATE - UNII:HPN8MZW13M) ALUMINUM CHLOROHYDRATE 12 mg in 100 g Inactive Ingredients Ingredient Name Strength MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) Product Characteristics Color white Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73306-1138-1 50 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 11/14/2022 
Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final M019 11/14/2022 Labeler - BASTON INDUSTRIA DE AEROSSOIS LTDA (897727605) Registrant - BASTON INDUSTRIA DE AEROSSOIS LTDA (897727605) Establishment Name Address ID/FEI Business Operations BASTON INDUSTRIA DE AEROSSOIS LTDA 897727605 manufacture(73306-1138)
