Label: SENSITIVE SKIN ANTIPERSPIRANT DEODORANT ROLL-ON JAFRA DAILY- aluminum chlorohydrate liquid
-
Contains inactivated NDC Code(s)
NDC Code(s): 68828-197-01, 68828-197-02 - Packager: Jafra cosmetics International
- 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 May 22, 2019
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
-
ACTIVE INGREDIENT
Active Ingredients Purpose
Aluminum Chlorohydrate 12.3 % Antiperspirant
Uses
reduces underarm wetness
keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Stop use if rash or irritation occur
Warnings
For external use only
Do not use on Broken Skin
Ask a doctor before use if you have kidney disease.
Directions
apply to underarms only
Inactive ingredients
Water/Aqua, PEG-40 Stearate, Stearic Acid, PEG-25 Propylene Glycol Stearate, Cetyl Alcohol, Magnesium Aluminum Silicate, Sorbitan Sesqiolate Phenoxyethanol, Ethylhexylglycerin, Thymus Vulgaris (Thyme) Oil, Lavandula Angustifolia (Lavender) Oil, Cedrus Atlantica (cedarleaf) Oil, Rosmarinus Officinalis (Rosemary) Oil, Geranium Maculatum Oil, Abies Alba (Fir Needle) Oil, Aniba Roseadora (Rosewood) Oil, Citrus Aurantium Bergamia (Bergamont) Oil, Cananga Odorata (Ylang Ylang) Oil.
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
SENSITIVE SKIN ANTIPERSPIRANT DEODORANT ROLL-ON JAFRA DAILY
aluminum chlorohydrate liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:68828-197 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (ALUMINUM CHLOROHYDRATE - UNII:HPN8MZW13M) ALUMINUM CHLOROHYDRATE 12.3 g in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) PEG-40 STEARATE (UNII: ECU18C66Q7) STEARIC ACID (UNII: 4ELV7Z65AP) PEG-25 PROPYLENE GLYCOL STEARATE (UNII: X21KPH4633) GLYCOL STEARATE (UNII: 0324G66D0E) CETYL ALCOHOL (UNII: 936JST6JCN) MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC) SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A) PHENOXYETHANOL (UNII: HIE492ZZ3T) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) THYME OIL (UNII: 2UK410MY6B) LAVENDER OIL (UNII: ZBP1YXW0H8) CEDAR LEAF OIL (UNII: BJ169U4NLG) ROSEMARY OIL (UNII: 8LGU7VM393) GERANIUM MACULATUM ROOT OIL (UNII: H2E371EDYX) ABIES ALBA LEAF OIL (UNII: G49QS877DA) ROSEWOOD OIL (UNII: F2522O5L7B) BERGAMOT OIL (UNII: 39W1PKE3JI) CANANGA OIL (UNII: 8YOY78GNNX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:68828-197-02 1 in 1 CARTON 09/02/2014 1 NDC:68828-197-01 60 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part350 09/02/2014 Labeler - Jafra cosmetics International (041676479) Registrant - Jafra cosmetics International (041676479) Establishment Name Address ID/FEI Business Operations Jafra Manufacturing, S.A. de C.V. 814732061 manufacture(68828-197)