Home NDC 70026-001-01 Yonis Bliss
Product NDC 70026-001
Requested package NDC 70026-001-01
11-digit product format 700260001
Labeler code 70026
Product ID 70026-001_eeb5d4f1-8cac-9ef6-e053-2a95a90a823f
Type HUMAN OTC DRUG
Nonproprietary name Chamomilla, Natrum Muriaticum
Dosage form GEL
Route TOPICAL
Labeler Brookhaus Essentials LLC
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2015-10-23
Substance MATRICARIA RECUTITA; SODIUM CHLORIDE
Active strength 6; 6 [hp_C]/g; [hp_C]/g
Pharmacologic classes Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Yonis Bliss
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MATRICARIA RECUTITA 6 [hp_C]/g SODIUM CHLORIDE 6 [hp_C]/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination G0R4UBI2ZZ Internal UNII lookup 451W47IQ8X Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 70026-001-01 Yonis Bliss 100 g in 1 BOTTLE, PUMP GEL 100 5
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded MATRICARIA RECUTITA ACTIVE INGREDIENT G0R4UBI2ZZ YONIS BLISS (CHAMOMILLA, NATRUM MURIATICUM) GEL [BROOKHAUS ESSENTIALS LLC] 1 SODIUM CHLORIDE ACTIVE INGREDIENT 451W47IQ8X YONIS BLISS (CHAMOMILLA, NATRUM MURIATICUM) GEL [BROOKHAUS ESSENTIALS LLC] 1 MATRICARIA RECUTITA ACTIVE MOIETY G0R4UBI2ZZ YONIS BLISS (CHAMOMILLA, NATRUM MURIATICUM) GEL [BROOKHAUS ESSENTIALS LLC] 1 SODIUM CATION ACTIVE MOIETY LYR4M0NH37 YONIS BLISS (CHAMOMILLA, NATRUM MURIATICUM) GEL [BROOKHAUS ESSENTIALS LLC] 1 ALOE VERA LEAF INACTIVE INGREDIENT ZY81Z83H0X YONIS BLISS (CHAMOMILLA, NATRUM MURIATICUM) GEL [BROOKHAUS ESSENTIALS LLC] 1 CARRAGEENAN INACTIVE INGREDIENT 5C69YCD2YJ YONIS BLISS (CHAMOMILLA, NATRUM MURIATICUM) GEL [BROOKHAUS ESSENTIALS LLC] 1 CITRIC ACID MONOHYDRATE INACTIVE INGREDIENT 2968PHW8QP YONIS BLISS (CHAMOMILLA, NATRUM MURIATICUM) GEL [BROOKHAUS ESSENTIALS LLC] 1 SODIUM BENZOATE INACTIVE INGREDIENT OJ245FE5EU YONIS BLISS (CHAMOMILLA, NATRUM MURIATICUM) GEL [BROOKHAUS ESSENTIALS LLC] 1 SODIUM HYDROXYMETHYLGLYCINATE INACTIVE INGREDIENT DIG6BWZ9XT YONIS BLISS (CHAMOMILLA, NATRUM MURIATICUM) GEL [BROOKHAUS ESSENTIALS LLC] 1 WATER INACTIVE INGREDIENT 059QF0KO0R YONIS BLISS (CHAMOMILLA, NATRUM MURIATICUM) GEL [BROOKHAUS ESSENTIALS LLC] 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 70026-001 YONIS BLISS (CHAMOMILLA, NATRUM MURIATICUM) GEL [BROOKHAUS ESSENTIALS LLC] 5 Current NDC, Legacy NDC, 1 package rows 20221202_ea4091d6-d295-41a0-aae5-68f3c260e110.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 70026-001-01 70026000101 100 g in 1 BOTTLE, PUMP (70026-001-01) 100 g 2015-10-23 0000-00-00 No No Current